Date published: 2025-11-4

1-800-457-3801

SCBT Portrait Logo
Seach Input

Arachidonoyl-N,N-dimethyl amide (CAS 45280-17-9)

0.0(0)
Write a reviewAsk a question

Alternate Names:
Arachidonic Acid-N,N-dimethyl amide
Application:
Arachidonoyl-N,N-dimethyl amide is a cell-cell communication inhibitor
CAS Number:
45280-17-9
Molecular Weight:
331.53
Molecular Formula:
C22H37NO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Arachidonoyl-N,N-dimethyl amide, identified by CAS number 45280-17-9, is a synthetic analog of arachidonic acid in which the carboxylic acid group is modified to an amide, specifically dimethylated at the nitrogen atom. This modification imparts distinct physical and chemical properties compared to its parent compound, arachidonic acid, a naturally occurring polyunsaturated fatty acid integral to the biosynthesis of eicosanoids. The structural alteration of transforming the acid group into an amide enhances the molecule′s lipophilicity and stability, making it particularly useful in research focused on lipid-mediated signaling pathways. Arachidonoyl-N,N-dimethyl amide is utilized in studies exploring the interaction of lipid molecules with protein targets, such as enzymes and receptors involved in signal transduction processes. By examining how this compound interacts with various cellular components, researchers can gain insights into the mechanisms by which lipid modifications influence cellular signaling and function. This work is crucial for understanding fundamental aspects of cell biology, such as how cells regulate responses to external stimuli through changes in lipid composition and structure. The research involving Arachidonoyl-N,N-dimethyl amide contributes to broader scientific knowledge, helping explain the non-medical roles of modified lipids in cellular systems across a range of biological contexts.


Arachidonoyl-N,N-dimethyl amide (CAS 45280-17-9) References

  1. Arachidonic acid amide inhibitors of gap junction cell-cell communication.  |  Boger, DL., et al. 1999. Bioorg Med Chem Lett. 9: 1151-4. PMID: 10328303
  2. Structural requirements for binding of anandamide-type compounds to the brain cannabinoid receptor.  |  Sheskin, T., et al. 1997. J Med Chem. 40: 659-67. PMID: 9057852

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Arachidonoyl-N,N-dimethyl amide, 5 mg

sc-205213
5 mg
$50.00

Arachidonoyl-N,N-dimethyl amide, 10 mg

sc-205213A
10 mg
$127.00